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The biological variation of insulin resistance markers: data from the European Biological Variation Study (EuBIVAS).
Carobene, Anna; Kilpatrick, Eric; Bartlett, William A; Fernández Calle, Pilar; Coskun, Abdurrahman; Díaz-Garzón, Jorge; Jonker, Niels; Locatelli, Massimo; Sandberg, Sverre; Aarsand, Aasne K.
Affiliation
  • Carobene A; Laboratory Medicine, 48455 IRCCS San Raffaele Scientific Institute , Milano, Italy.
  • Kilpatrick E; Sidra Medicine, Doha, Qatar.
  • Bartlett WA; School of Medicine, University of Dundee, Dundee, Scotland, UK.
  • Fernández Calle P; Department of Laboratory Medicine, Hospital Universitario La Paz, Madrid, Spain.
  • Coskun A; School of Medicine, Acibadem Mehmet Ali Aydinlar University, Istanbul, Türkiye.
  • Díaz-Garzón J; Department of Laboratory Medicine, Hospital Universitario La Paz, Madrid, Spain.
  • Jonker N; Certe, Wilhelmina Ziekenhuis Assen, Assen, The Netherlands.
  • Locatelli M; Laboratory Medicine, 48455 IRCCS San Raffaele Scientific Institute , Milano, Italy.
  • Sandberg S; Norwegian Porphyria Centre, Department of Medical Biochemistry and Pharmacology, Haukeland University Hospital, Bergen, Norway.
  • Aarsand AK; Norwegian Organization for Quality Improvement of Laboratory Examinations (Noklus), Haraldsplass Deaconess Hospital, Bergen, Norway.
Clin Chem Lab Med ; 2024 Jul 12.
Article in En | MEDLINE | ID: mdl-38987271
ABSTRACT

OBJECTIVES:

An insulin resistant state is characteristic of patients with type 2 diabetes, polycystic ovary syndrome, and metabolic syndrome. Identification of insulin resistance (IR) is most readily achievable using formulae combining plasma insulin and glucose results. In this study, we have used data from the European Biological Variation Study (EuBIVAS) to examine the biological variability (BV) of IR using the Homeostasis Model Assessment for Insulin Resistance (HOMA-IR) and the Quantitative Insulin sensitivity Check Index (QUICKI).

METHODS:

Ninety EuBIVAS non-diabetic subjects (52F, 38M) from five countries had fasting HOMA-IR and QUICKI calculated from plasma glucose and insulin samples collected concurrently on 10 weekly occasions. The within-subject (CVI) and between-subject (CVG) BV estimates with 95 % CIs were obtained by CV-ANOVA after analysis of trends, variance homogeneity and outlier removal.

RESULTS:

The CVI of HOMA-IR was 26.7 % (95 % CI 25.5-28.3), driven largely by variability in plasma insulin and the CVI for QUICKI was 4.1 % (95 % CI 3.9-4.3), reflecting this formula's logarithmic transformation of glucose and insulin values. No differences in values or BV components were observed between subgroups of men or women below and above 50 years.

CONCLUSIONS:

The EuBIVAS, by utilising a rigorous experimental protocol, has produced robust BV estimates for two of the most commonly used markers of insulin resistance in non-diabetic subjects. This has shown that HOMA-IR, in particular, is highly variable in the same individual which limits the value of single measurements.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Clin Chem Lab Med Journal subject: QUIMICA CLINICA / TECNICAS E PROCEDIMENTOS DE LABORATORIO Year: 2024 Type: Article Affiliation country: Italy

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Clin Chem Lab Med Journal subject: QUIMICA CLINICA / TECNICAS E PROCEDIMENTOS DE LABORATORIO Year: 2024 Type: Article Affiliation country: Italy